IP Library Granted Patent US 12,302,933
Granted Patent B2
US 12,302,933 · App. 17/848,345 · Granted May 20, 2025

Flavor delivery system

Inventor: Jiten Dihora (Center Valley, PA)
Assignee: TRUCAPSOL LLC
A23L27/10A23J3/227A23P30/20A61K8/922A61Q11/00A23V2002/00
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Quick Facts
Patent No.
US 12,302,933
App. No.
17/848,345
Granted
May 20, 2025
Kind
B2
Abstract

Disclosed are controlled release particles including: (a) a flavor oil; (b) a plant derived fat; (c) a plant derived wax; (d) a plant derived surfactant; and (e) optionally an anti-oxidant. The particles are particularly useful as a flavor delivery system of a personal care product, an oral care product, a powdered food product, a fluid food product, a powdered nutritional supplement, a fluid nutritional supplement, a bakery dough, a dairy product, a savory food product, a noodle bowl and a non-animal based meat analogue.

Claims (21)

1. A controlled release particle consisting of the following components: (a) a flavor oil; (b) a plant derived fat; (c) a plant derived wax; (d) a plant derived surfactant; and (e) optionally an anti-oxidant, wherein the components are homogeneously distributed throughout the controlled release particle.

2. The controlled release particle of claim 1 , consisting of 5-35 wt. % of the flavor oil; 40-67 wt. % of the plant derived fat; 18-40 wt. % of the plant derived wax; 0.2-2 wt. % of the plant derived surfactant; and optionally 0-2% of the anti-oxidant.

3. The controlled release particle of claim 1 , wherein the flavor oil is at least one member selected from the group consisting of plant extracts, fruit extracts, artificial flavors, essential oils, flavor enhancers, and flavors that mimic meat flavors.

4. The controlled release particle of claim 1 , wherein the plant derived fat is based on at least one member selected from the group consisting of coconut, palm, cocoa, illip, shea, avocado, jojoba, sunflower, almond, rice, tea and vegerite.

5. The controlled release particle of claim 1 , wherein the plant derived wax is at least one member selected from the group consisting of floral waxes, hydrogenated oil waxes, candelilla wax, carnauba wax, berry wax, fruit wax, sunflower wax, rice bran wax, and fatty alcohols.

6. The controlled release particle of claim 1 , wherein the anti-oxidant is at least one member selected from the group consisting of Vitamin A, Vitamin C, Vitamin E, folic acid, Beta-carotene, Coenzyme Q10, alpha-tocopherol and polyphenols.

7. The controlled release particle of claim 1 , wherein the plant derived surfactant is selected from the group consisting of plant extracts, glucosides, lecithins, de-oiled lecithins and mixtures thereof.

8. The controlled release particle of claim 1 , which has a diameter from 100 microns to less than 5000 microns.

9. A composition comprising a plurality of the controlled release particle of claim 1 , wherein the composition is a personal care product, an oral care product, a powdered food product, a fluid food product, a powdered nutritional supplement, a fluid nutritional supplement, a bakery dough, a dairy product, a savory food product, a noodle bowl or a non-animal based meat analogue.

10. The composition of claim 9 , which is configured to release a first flavor composition using a first controlled release technology and to release a second flavor composition different from the first flavor composition using a second controlled release technology different from the first controlled release technology, wherein the first controlled release technology and the second controlled release technology are selected from the group consisting of neat oils, water-triggered release flavor delivery systems, and heat-triggered release flavor delivery systems.

11. A method for preparing the controlled release particle of claim 1 , said method comprising:

heating the plant derived fat and the plant derived wax above melting temperatures thereof to provide a first mixture;

mixing the plant derived surfactant and the flavor oil at room temperature and heating to 50° C. in a sealed container to provide a second mixture;

dispersing the second mixture into the first mixture to obtain a homogeneous solution;

mechanically manipulating the homogeneous solution to provide droplets or extrudates of a desired shape and a desired size; and

cooling the formed droplets or extrudates to ambient temperature to provide the controlled release particle.

12. The method of claim 11 , wherein the mechanical manipulating comprises extrusion, prilling and atomization followed by coating onto an edible food product, pastille making using a cooled drum, 3D printing, sheet forming followed by cutting, dividing, or grinding into a plurality of desired sized particles.

13. A method for preparing a finished product composition comprising a plurality of the controlled release particle of claim 1 as a flavor delivery system, said method comprising the steps of:

mixing the plurality of the controlled release particle with other components of the finished product composition to deliver 0.001 to 0.75 grams of flavor per gram of the finished product composition; and

forming the finished product composition via hand molding, automated molding, baking, freezing, frying, extruding, or mixing/blending.

14. The controlled release particle of claim 1 , wherein the flavor oil mimics meat flavors and is provided in an amount from 5 to 35 wt. % of the controlled release particle.

Assignments (2)
SECURITY INTEREST Recorded Sep 25, 2023
From: TRUCAPSOL LLC
To: ALTER DOMUS (US) LLC
Reel/Frame 065010/0311 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 23, 2022
From: DIHORA, JITEN
To: TRUCAPSOL LLC
Reel/Frame 060298/0086 →
Continuity (2)
Provisional Application 63215169 · Jun 25, 2021
Related Publication 20220408771A1 · Dec 29, 2022
References Cited (130)
US 2573900A · Freeman · 1951 [cited by examiner]
US 3345358A · Inklaar · 1967 [cited by applicant]
US 3819838A · Smith et al. · 1974 [cited by applicant]
US 3870542A · Ida et al. · 1975 [cited by applicant]
US 3943949A · Ashton · 1976 [cited by examiner]
US 4076774A · Short · 1978 [cited by applicant]
US 4626471A · Chao · 1986 [cited by applicant]
US 4752485A · Sharma · 1988 [cited by examiner]
US 4818539A · Shaw · 1989 [cited by examiner]
US 5015527A · Chao · 1991 [cited by applicant]
US 5126151A · Bodor · 1992 [cited by examiner]
US 5227446A · Denzinger et al. · 1993 [cited by applicant]
US 5431930A · Patel · 1995 [cited by examiner]
US 5550189A · Qin et al. · 1996 [cited by applicant]
US 5574179A · Wahl et al. · 1996 [cited by applicant]
US 5601760A · Rosenberg · 1997 [cited by applicant]
US 5837747A · Soon-Shiong et al. · 1998 [cited by applicant]
US 6248909B1 · Akimoto et al. · 2001 [cited by applicant]
US 6465016B2 · Parikh et al. · 2002 [cited by applicant]
US 6572919B2 · Westland et al. · 2003 [cited by applicant]
US 6596073B1 · Nyssen et al. · 2003 [cited by applicant]
US 6855335B2 · Seok et al. · 2005 [cited by applicant]
US 7431986B2 · Van Lengerich et al. · 2008 [cited by applicant]
US 8900495B2 · Pacorel et al. · 2014 [cited by applicant]
US 8993041B2 · To et al. · 2015 [cited by applicant]
US 9205395B2 · Yan · 2015 [cited by applicant]
US 9332774B2 · Nakhasi et al. · 2016 [cited by applicant]
US 9416050B2 · Seidl et al. · 2016 [cited by applicant]
US 9427719B2 · Viaud-Massuard et al. · 2016 [cited by applicant]
US 9714397B2 · Feng et al. · 2017 [cited by applicant]
US 9937477B2 · Zhang et al. · 2018 [cited by applicant]
US 9944886B2 · Hitchcock et al. · 2018 [cited by applicant]
US 9993401B2 · Barnett et al. · 2018 [cited by applicant]
US 10188593B2 · Dihora et al. · 2019 [cited by applicant]
US 11179302B2 · Dardelle · 2021 [cited by applicant]
US 11344502B1 · Dihora et al. · 2022 [cited by applicant]
US 11465117B2 · Bachawala et al. · 2022 [cited by applicant]
US 11484857B2 · Bachawala et al. · 2022 [cited by applicant]
US 11542392B1 · Multari · 2023 [cited by applicant]
US 11547978B2 · Bachawala et al. · 2023 [cited by applicant]
US 11571674B1 · Dihora et al. · 2023 [cited by applicant]
US 20020169233A1 · Schwantes · 2002 [cited by applicant]
US 20040017017A1 · Van Lengerich et al. · 2004 [cited by applicant]
US 20040033264A1 · Sawhney · 2004 [cited by applicant]
US 20050272628A1 · Meli et al. · 2005 [cited by applicant]
US 20050276831A1 · Dihora et al. · 2005 [cited by applicant]
US 20070122455A1 · Myers · 2007 [cited by examiner]
US 20080085297A1 · Dave et al. · 2008 [cited by applicant]
US 20080103265A1 · Schocker et al. · 2008 [cited by applicant]
US 20080167188A1 · Fischer et al. · 2008 [cited by applicant]
US 20090209661A1 · Somerville Roberts et al. · 2009 [cited by applicant]
US 20100011610A1 · Bittorf et al. · 2010 [cited by applicant]
US 20100028451A1 · Kaplan et al. · 2010 [cited by applicant]
US 20110052680A1 · Hendrickson et al. · 2011 [cited by applicant]
US 20110268778A1 · Dihora et al. · 2011 [cited by applicant]
US 20110268802A1 · Dihora et al. · 2011 [cited by applicant]
US 20120128752A1 · Loo et al. · 2012 [cited by applicant]
US 20130004617A1 · Zhang et al. · 2013 [cited by applicant]
US 20130022654A1 · Deshmukh et al. · 2013 [cited by applicant]
US 20130084379A1 · Gregson et al. · 2013 [cited by applicant]
US 20130239429A1 · Vella et al. · 2013 [cited by applicant]
US 20140199244A1 · Rijcken et al. · 2014 [cited by applicant]
US 20140335032A1 · Panandiker et al. · 2014 [cited by applicant]
US 20150252312A1 · De Villeneuve et al. · 2015 [cited by applicant]
US 20160038428A1 · Harel et al. · 2016 [cited by applicant]
US 20160128944A1 · Chawrai et al. · 2016 [cited by applicant]
US 20160158121A1 · Lei et al. · 2016 [cited by applicant]
US 20160166480A1 · Lei et al. · 2016 [cited by applicant]
US 20160206561A1 · Kohane et al. · 2016 [cited by applicant]
US 20160228338A9 · Dihora et al. · 2016 [cited by applicant]
US 20170165627A1 · Duan et al. · 2017 [cited by applicant]
US 20180015009A1 · Soubiran et al. · 2018 [cited by applicant]
US 20180042825A1 · Lei et al. · 2018 [cited by applicant]
US 20190275490A1 · Bachawala · 2019 [cited by applicant]
US 20210045409A1 · Witteveen et al. · 2021 [cited by applicant]
US 20220133603A1 · Bachawala et al. · 2022 [cited by applicant]
US 20230060181A1 · Dihora et al. · 2023 [cited by applicant]
CA 1049335A · 1979 [cited by applicant]
CN 114539887A · 2022 [cited by applicant]
EP 0076515A1 · 1983 [cited by applicant]
EP 0361677B2 · 1993 [cited by applicant]
EP 0815743A2 · 1998 [cited by applicant]
EP 1371410A1 · 2003 [cited by applicant]
EP 1797946A2 · 2007 [cited by applicant]
GB 2363964A · 2002 [cited by examiner]
JP H0284147A · 1990 [cited by examiner]
RU 2351364C2 · 2009 [cited by examiner]
WO 9901214A1 · 1999 [cited by applicant]
WO 0105926A1 · 2001 [cited by applicant]
WO 03013538A1 · 2003 [cited by applicant]
WO 2004064971A2 · 2004 [cited by applicant]
WO WO2006024411A2 · 2006 [cited by applicant]
WO 2007135583A2 · 2007 [cited by applicant]
WO 2008118133A2 · 2008 [cited by applicant]
WO WO2009098226A1 · 2009 [cited by applicant]
WO 2011041395A2 · 2011 [cited by applicant]
WO 2015091877A1 · 2015 [cited by applicant]
WO 2016071151A1 · 2016 [cited by applicant]
WO 2017023830A1 · 2017 [cited by applicant]
WO WO2020195132A1 · 2020 [cited by applicant]
NPL Diglyceride (Retrieved on Jan. 28, 2025). (Year: 2025). [cited by examiner]
NPL Glyceride (Retrieved on Jan. 28, 2025). (Year: 2025). [cited by examiner]
U.S. Appl. No. 16/287,509, filed Feb. 27, 2019. [cited by applicant]
U.S. Appl. No. 16/682,862, filed Nov. 13, 2019. [cited by applicant]
U.S. Appl. No. 16/830,152, filed Mar. 25, 2020. [cited by applicant]
U.S. Appl. No. 16/853,003, filed Apr. 20, 2020. [cited by applicant]
U.S. Appl. No. 17/517,816, filed Nov. 3, 2021. [cited by applicant]
U.S. Appl. No. 16/776,828, filed Jan. 30, 2020. [cited by applicant]
U.S. Appl. No. 16/776,965, filed Jan. 30, 2020. [cited by applicant]
U.S. Appl. No. 16/777,048, filed Jan. 30, 2020. [cited by applicant]
U.S. Appl. No. 17/724,141, filed Apr. 19, 2022. [cited by applicant]
U.S. Appl. No. 17/724,166, filed Apr. 19, 2022. [cited by applicant]
Jardine. (2022). Amino-functionalized polysaccharide derivatives: Synthesis, properties and application. Current Research in Green and Sustainable Chemistry 5, 100309. [cited by applicant]
Gasparini et al. (2020). Quantification of residual perfume by Py-GC-MS in fragrance encapsulate polymeric materials intended for biodegradation tests. Molecules, 25, 718. [cited by applicant]
Larson et al. (2017). Bulky polar additives that greatly reduce the viscosity of concentrated solutions of therapeutic monoclonal antibodies. Journal of Pharmaceutical Sciences, 106, 1211-1217. [cited by applicant]
Guo et al. (2012). Structure-activity relationship for hydrophobic salts as viscosity-lowering excipients for concentrated solutions of monoclonal antibodies. Pharm Res, 3102-3109. [cited by applicant]
Kumar et al. (2017). Viscosity-reducing bulky-salt excipients prevent gelation of protein, but not carbohydrate, solutions. Appl Biochem Biotechnol, 1491-1496. [cited by applicant]
Wang et al. (2021). Hofmeister effect on the viscosity properties of gelatin in dilute solutions. Colloids and Surfaces B: Biointerfaces, 206, 111944. [cited by applicant]
OECD 301D method (OECD 1992, Test No. 301 Ready Biodegradability, OECD Guidelines for the Testing of Chemicals, Section 3, OECD Publishing, Paris, https://doi.org/10.1787/9789264070349-en. [cited by applicant]
Thakore et al. (2001). “Studies on biodegradability, morphology and thermo-mechanical properties of LDPE/ modified starch blends.” European polymer journal, 37(1), 151-160. [cited by applicant]
Adhesives Magazine (2016). SARTOMER: Acrylate Oliogmer. Available at: https://www.adhesivesmag.com/articles/94922-sartomer-acrylate-oligomer. [cited by applicant]
Leung et al. (2017). Enteric coating of micron-size drug particles through a Würster fluid-bed process. Powder Technology, 317, 247-252. [cited by applicant]
Luo et al. (2014). Zein-based micro-and nano-particles for drug and nutrient delivery: A review. Journal of Applied Polymer Science, 131(16): 40696, 1-12. [cited by applicant]
Silverajah et al. (2012). Mechanical, thermal and morphological properties of poly (lactic acid)/epoxidized palm olein blend. Molecules, 17(10), 11729-11747. [cited by applicant]
Tmakova et al. (2015). Plant-derived surfactants as an alternative to synthetic surfactants: surface and antioxidant activities. Chemical Papers, 70(2), 188-196. [cited by applicant]
Werner et al. (2007). Air-suspension particle coating in the food industry: Part I—State of the art. Powder Technology, 171(1), 25-33. [cited by applicant]
English language abstract for WO 2009098226 A1 (2009). [cited by applicant]
English language abstract for WO 2020195132 A1 (2020). [cited by applicant]
http://polymerdatabase.com/polymer%20physics/sigma.html downloaded on Apr. 29, 2022. [cited by applicant]
Ko et al., “Characterization of hydrophilic-hydrophobic polymeric surfaces by contact angle measurements”, Journal of Colloid and Interface Science, vol. 82(1) (1981). [cited by applicant]
Cited By (1)
US 12,723,125